Evidence map›Paper›PMID 35367209›Full record

ArticleThe Journal of biological chemistry2022

Mitochondria-associated myosin 19 processively transports mitochondria on actin tracks in living cells.

Osamu Sato, Tsuyoshi Sakai, Young-Yeon Choo, Reiko Ikebe, Tomonobu M Watanabe, Mitsuo Ikebe

Open access · goldAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Prenylcysteine Oxidase 1 Deficiency Protects the Cardiac Muscle Cell Line HL-1 Against Ischaemic/Hypoxic Stress.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. A novel, rapidly progressive ataxia due to a spontaneous Myo5a mutation in mice impairs transport proteins and alters mitochondria.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. The multiple links between actin and mitochondria.Nature reviews. Molecular cell biology · 2023
    Review
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Osamu SatoDepartment of Cellular and Molecular Biology, University of Texas at Tyler Health Science Center, Tyler, Texas, USA.
Tsuyoshi SakaiDepartment of Cellular and Molecular Biology, University of Texas at Tyler Health Science Center, Tyler, Texas, USA.
Young-Yeon ChooDepartment of Cellular and Molecular Biology, University of Texas at Tyler Health Science Center, Tyler, Texas, USA.
Reiko IkebeDepartment of Cellular and Molecular Biology, University of Texas at Tyler Health Science Center, Tyler, Texas, USA.
Tomonobu M WatanabeLaboratory for Comprehensive Bioimaging, RIKEN Center for Biosystems Dynamics Research, Kobe, Hyogo, Japan.
Mitsuo IkebeDepartment of Cellular and Molecular Biology, University of Texas at Tyler Health Science Center, Tyler, Texas, USA. Electronic address: Mitsuo.Ikebe@uthct.edu.
The University of Texas Health Science Center at Tyler · USRIKEN Center for Biosystems Dynamics Research · JP

Funding

Myocardin in the pathogenesis of pleural remodelingR01HL142853 · NHLBI · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI IDELL, STEVEN, IKEBE, MITSUO · 2019 to 2022
$1.9M
NHLBI NIH HHS R01 HL142853
6 · The paper itself

Abstract

Mitochondria are fundamentally important in cell function, and their malfunction can cause the development of cancer, cardiovascular disease, and neuronal disorders. Myosin 19 (Myo19) shows discrete localization with mitochondria and is thought to play an important role in mitochondrial dynamics and function; however, the function of Myo19 in mitochondrial dynamics at the cellular and molecular levels is poorly understood. Critical missing information is whether Myo19 is a processive motor that is suitable for transportation of mitochondria. Here, we show for the first time that single Myo19 molecules processively move on actin filaments and can transport mitochondria in cells. We demonstrate that Myo19 dimers having a leucine zipper processively moved on cellular actin tracks in demembraned cells with a velocity of 50 to 60 nm/s and a run length of ∼0.4 μm, similar to the movement of isolated mitochondria from Myo19 dimer-transfected cells on actin tracks, suggesting that the Myo19 dimer can transport mitochondria. Furthermore, we show single molecules of Myo19 dimers processively moved on single actin filaments with a large step size of ∼34 nm. Importantly, WT Myo19 single molecules without the leucine zipper processively move in filopodia in living cells similar to Myo19 dimers, whereas deletion of the tail domain abolished such active movement. These results suggest that Myo19 can processively move on actin filaments when two Myo19 monomers form a dimer, presumably as a result of tail-tail association. In conclusion, Myo19 molecules can directly transport mitochondria on actin tracks within living cells.

Indexed as

ActinsMyosinsActin CytoskeletonMitochondriaMitochondrial DynamicsPseudopodiaActinsMyosinsintracellular movementmitochondriasingle moleculeTIRF microscopyunconventional myosin

Identifiers

PMID35367209
PMCPMC9065997
OpenAlexW4221130511

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.